The Aspergillus Genome Database: multispecies curation and incorporation of RNA-Seq data to improve structural gene annotations

被引:209
作者
Cerqueira, Gustavo C. [1 ]
Arnaud, Martha B. [2 ]
Inglis, Diane O. [2 ]
Skrzypek, Marek S. [2 ]
Binkley, Gail [2 ]
Simison, Matt [2 ]
Miyasato, Stuart R. [2 ]
Binkley, Jonathan [2 ]
Orvis, Joshua [3 ]
Shah, Prachi [2 ]
Wymore, Farrell [2 ]
Sherlock, Gavin [2 ]
Wortman, Jennifer R. [1 ]
机构
[1] Broad Inst Harvard & MIT, Cambridge, MA 02141 USA
[2] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[3] Univ Maryland, Sch Med, Inst Genome Sci, Baltimore, MD 21201 USA
基金
美国国家卫生研究院;
关键词
ORYZAE; FUMIGATUS; TRANSCRIPTOME; NIDULANS; BROWSER; NIGER;
D O I
10.1093/nar/gkt1029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The Aspergillus Genome Database (AspGD; http://www.aspgd.org) is a freely available web-based resource that was designed for Aspergillus researchers and is also a valuable source of information for the entire fungal research community. In addition to being a repository and central point of access to genome, transcriptome and polymorphism data, AspGD hosts a comprehensive comparative genomics toolbox that facilitates the exploration of precomputed orthologs among the 20 currently available Aspergillus genomes. AspGD curators perform gene product annotation based on review of the literature for four key Aspergillus species: Aspergillus nidulans, Aspergillus oryzae, Aspergillus fumigatus and Aspergillus niger. We have iteratively improved the structural annotation of Aspergillus genomes through the analysis of publicly available transcription data, mostly expressed sequenced tags, as described in a previous NAR Database article (Arnaud et al. 2012). In this update, we report substantive structural annotation improvements for A. nidulans, A. oryzae and A. fumigatus genomes based on recently available RNA-Seq data. Over 26 000 loci were updated across these species; although those primarily comprise the addition and extension of untranslated regions (UTRs), the new analysis also enabled over 1000 modifications affecting the coding sequence of genes in each target genome.
引用
收藏
页码:D705 / D710
页数:6
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